Discover our
main three areas
of interest
CMC Consulting
We ensure compliance with regulatory standards, optimize product development, and enhance manufacturing processes, ultimately leading to high-quality, safe, and effective biopharmaceutical products.
Qualification & Validation
Our service focus includes document creation for compliance, risk-based project management to enhance quality and safety, and GMP-upgrades to ensure facilities meet evolving regulations and adapt to product changes.
Bioprocessing & PAT
We help our clients streamline bioprocesses to reduce costs and improve quality, all tailored to their needs. Our tool, EDDI, provides complete cell data for precise characterization, eliminating guesswork and enabling informed decisions.
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